Cecilia W. Lo

Novel Jbts17 mutant mouse model of Joubert syndrome with cilia transition zone defects and cerebellar and other ciliopathy related anomalies.

Establishing normative nasal nitric oxide values in infants.

Automated identification of abnormal respiratory ciliary motion in nasal biopsies.

Prickle1 mutation causes planar cell polarity and directional cell migration defects associated with cardiac outflow tract anomalies and other structural birth defects.

Brain Dysplasia Associated with Ciliary Dysfunction in Infants with Congenital Heart Disease.

Cilia and Ciliopathies in Congenital Heart Disease.

Reply.

Assessment of ciliary phenotype in primary ciliary dyskinesia by micro-optical coherence tomography.

The complex genetics of hypoplastic left heart syndrome.

Phenotyping cardiac and structural birth defects in fetal and newborn mice.

Diverse application of MRI for mouse phenotyping.

Loss of function in is associated with tetralogy of Fallot and septal defects.

Airway ciliary dysfunction: Association with adverse postoperative outcomes in nonheterotaxy congenital heart disease patients.

Low Nasal NO in Congenital Heart Disease With Systemic Right Ventricle and Postcardiac Transplantation.

Airway ciliary dysfunction and respiratory symptoms in patients with transposition of the great arteries.

Wdpcp promotes epicardial EMT and epicardium-derived cell migration to facilitate coronary artery remodeling.

The Genetic Landscape of Hypoplastic Left Heart Syndrome.

A computational framework for the detection of subcortical brain dysmaturation in neonatal MRI using 3D Convolutional Neural Networks.

Congenital Heart Defects and Ciliopathies Associated With Renal Phenotypes.

Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6.

Vertebrate myosin 1d regulates left-right organizer morphogenesis and laterality.

Cardiac Targeting Peptide, a Novel Cardiac Vector: Studies in Bio-Distribution, Imaging Application, and Mechanism of Transduction.

Reply to 'Double-outlet right ventricle is not hypoplastic left heart syndrome'.

Deposition studies of aerosol delivery by nasal cannula to infants.

Left-right patterning in congenital heart disease beyond heterotaxy.

Role of cilia in the pathogenesis of congenital heart disease.

Mutation of LRP1 in cardiac neural crest cells causes congenital heart defects by perturbing outflow lengthening.

Rapid Ex-Vivo Ciliogenesis and Dose-Dependent Effect of Notch Inhibition on Ciliogenesis of Respiratory Epithelia.

A Membrane-Tethered Ubiquitination Pathway Regulates Hedgehog Signaling and Heart Development.

Cilia interactome with predicted protein-protein interactions reveals connections to Alzheimer's disease, aging and other neuropsychiatric processes.

Differential effect of anesthetics on mucociliary clearance in vivo in mice.

Mucociliary Clearance Scans Show Infants Undergoing Congenital Cardiac Surgery Have Poor Airway Clearance Function.

Cardiovascular Development and Congenital Heart Disease Modeling in the Pig.

Mechanisms of Impaired Lung Development and Ciliation in Mannosidase-1-Alpha-2 () Mutants.

Novel insights into the genetic landscape of congenital heart disease with systems genetics.

Gene-teratogen interactions influence the penetrance of birth defects by altering Hedgehog signaling strength.

Mitochondrial Respiration Defects in Single-Ventricle Congenital Heart Disease.

Relationships Between Regional Cerebral Blood Flow and Neurocognitive Outcomes in Children and Adolescents With Congenital Heart Disease.

Common deletion variants causing protocadherin-α deficiency contribute to the complex genetics of BAV and left-sided congenital heart disease.

Biallelic pathogenic variants in roundabout guidance receptor 1 associate with syndromic congenital anomalies of the kidney and urinary tract.

Genetic resiliency associated with dominant lethal mutation causing atrial septal defect with high heritability.

Cerebellar and Prefrontal Structures Associated With Executive Functioning in Pediatric Patients With Congenital Heart Defects.

Uncompensated mitochondrial oxidative stress underlies heart failure in an iPSC-derived model of congenital heart disease.

Novel Protein-Protein Interactions Highlighting the Crosstalk between Hypoplastic Left Heart Syndrome, Ciliopathies and Neurodevelopmental Delays.

Rare and Common Variants Uncover the Role of the Atria in Coarctation of the Aorta.

Flow blockage disrupts cilia-driven fluid transport in the epileptic brain.

Impaired Neurovascular Function Underlies Poor Neurocognitive Outcomes and Is Associated with Nitric Oxide Bioavailability in Congenital Heart Disease.

Profiling development of abdominal organs in the pig.

Correction to: Flow blockage disrupts cilia-driven fluid transport in the epileptic brain.

Clinical factors associated with microstructural connectome related brain dysmaturation in term neonates with congenital heart disease.